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LC-OCT can help identify lupus-related scarring hair loss by spotting unique features.

Sox13 is a marker for early hair follicle development but not essential for skin and hair growth.

Trps1 plays a key role in hair follicle development and cycling.

Truncated LTBP-1 disrupts TGF-beta signaling, affecting hair growth.

A newly found RNA in Cashmere goats may play a role in hair growth and development.

The transgenic safflower oil with oleosin-rhFGF9 improved hair growth and wound healing in mice.

Foxi3 expression in developing teeth and hair is controlled by the ectodysplasin pathway.

ALX4 is crucial for normal craniofacial and hair development, with specific roles in different cell types.

LHX2, with other markers, can identify hair placodes in rats.

TET enzymes are important for skin and hair development by controlling gene activity in specific areas.

The S250C variant in a gene may cause autoimmunity and immunodeficiency by impairing protein function.

LRIG1 protein affects hair growth by regulating skin receptors, leading to hair loss when overexpressed.

A clinically suspected melanoma appeared benign under the microscope but was confirmed by specific tests and a rare mutation.

A rare skin condition in a boy is likely due to a specific genetic mutation pattern.

TCF/Lef1 is essential for skin barrier function by regulating lipid metabolism.

Hox genes control hair growth patterns in mammals by regulating stem cell activity in the skin.

The human type II 5α-reductase gene, linked to certain male health conditions, has a specific structure and low similarity to other related genes.

New LPA receptors (LPA4, LPA5, LPA6) have diverse roles in the body.

Carriers of a specific gene mutation have subtle skin changes without visible symptoms.

VEGF and microvessel density are closely linked and peak during specific hair growth phases in cashmere goats.

Cats with abnormal hair had DSG4 gene changes causing hair problems.

A specific gene mutation causes different hair defects in Indian monilethrix families.

A gene mutation causes monilethrix in a Chinese family.

The Trichodysplasia spinulosa virus protein can cause abnormal hair growth in mice.

TCF/Lef1 activity is essential for proper skin cell development and renewal.

The study identified key genes and pathways that influence goat wool quality and growth.

Long-read RNA sequencing can identify complex gene changes in IFAP syndrome.

Folliculin deficiency causes problems with cell division and positioning due to disrupted RhoA signaling and interaction with p0071.

Certain genetic changes in the LSS gene cause a rare skin and hair condition.